Fungicide n-cycloalkyl-n-bicyclic-carboxamide derivatives

ABSTRACT

The present invention relates N-cycloalkyl-N-bicyclic-carboxamide, thiocarboxamide or N-substituted carboximidamide derivatives of formula (I) wherein A represents a carbo-linked, 5-membered heterocyclyl group; T represents O, S, N-R a , N—OR a , N—NR a R b  or N—CN; Z 1  represents a C 3 -C 7 -cycloalkyl group; X represents N or a CZ 7  and Z 2 ; Z 3 ; L 1  and L 2  represent various substituents; their process of preparation; preparation intermediate compounds; their use as fungicide active agents, particularly in the form of fungicide compositions and methods for the control of phytopathogenic fungi, notably of plants, using these compounds or compositions.

The present invention relates to N-cycloalkyl-N-bicyclic-carboxamide, thiocarboxamide or N-substituted carboximidamide derivatives, their process of preparation, preparation intermediate compounds, their use as fungicide active agents, particularly in the form of fungicide compositions, and methods for the control of phytopathogenic fungi, notably of plants, using these compounds or compositions.

In international patent application WO-2007/014290 certain N-substituted-N-bicyclic-carboxamide or thiocarboxamide derivatives are generically embraced in a broad disclosure of numerous compounds of the following formula:

wherein W¹ can represent oxygen or sulphur; A can represent NH or CH₂; R¹ can represent a phenyl or heterocyclic ring; G can represent a 5-membered heterocyclic ring, more specifically a thiazole ring; W² can represent oxygen or sulphur; Q^(a) can represent C₄-C₇-cycloalkyl and Q^(b) can represent a 8-11-membered, partially saturated, bicyclic system. However, this document does not specifically disclose nor suggest to select such compounds wherein the nitrogen atom of the N-Q^(a)Q^(b) moiety can be substituted by a cycloalkyl.

It is always of high-interest in agriculture to use novel pesticide compounds in order to avoid or to control the development of resistant strains to the active ingredients. It is also of high-interest to use novel compounds being more active than those already known, with the aim of decreasing the amounts of active compound to be used, whilst at the same time maintaining effectiveness at least equivalent to the already known compounds. We have now found a new family of compounds that possess the above mentioned effects or advantages.

Accordingly, the present invention provides N-cycloalkyl-N-bicyclic-carboxamide derivatives of formula (I)

wherein

-   -   A represents a carbo-linked, partially saturated or unsaturated,         5-membered heterocyclyl group that can be substituted by up to         four groups R;     -   T represents O, S, N—R^(a), N—OR^(a), N—NR^(a)R^(b) or N—CN;     -   Z¹ represents a non substituted C₃-C₇-cycloalkyl or a C₃-C₇         cycloalkyl substituted by up to 10 atoms or groups that can be         the same or different and that can be selected in the list         consisting of halogen atoms; cyano; C₁-C₈-alkyl;         C₁-C₈-halogenoalkyl comprising up to 9 halogen atoms that can be         the same or different; C₁-C₈-alkoxy; C₁-C₈-halogenoalkoxy         comprising up to 9 halogen atoms that can be the same or         different; C₁-C₈-alkoxycarbonyl; C₁-C₈-halogenoalkoxycarbonyl         comprising up to 9 halogen atoms that can be the same or         different; C₁-C₈-alkylaminocarbonyl; di-C₁-C₈-alkylaminocarbonyl         or carbamoyl;     -   Z² represents a hydrogen atom; a halogen atom; cyano;         C₁-C₈-alkyl; C₁-C₈-halogenoalkyl comprising up to 9 halogen         atoms that can be the same or different;     -   L¹ and L², that can be the same or different, represent CZ⁴Z⁵,         NZ⁶, O, S, S(O) or S(O)₂;     -   m represents 1, 2 or 3;     -   X represents CZ⁷ or N;     -   Z³ and Z⁷, that can be the same or different, represent a         hydrogen atom; a halogen atom; nitro; cyano; hydroxyl; thio;         amino; pentafluoro-A6-thio; C₁-C₈-alkyl; C₁-C₈-halogenoalkyl         comprising up to 9 halogen atoms that can be the same or         different; C₁-C₈-alkylamino; di-C₁-C₈-alkylamino; C₁-C₈-alkoxy;         C₁-C₈-halogenoalkoxy comprising up to 9 halogen atoms that can         be the same or different; C₁-C₈-alkoxy-C₁-C₈-alkyl;         C₁-C₈-alkylsulphanyl; C₁-C₈-halogenoalkylsulphanyl comprising up         to 9 halogen atoms that can be the same or different;         C₂-C₈-alkenyl; C₂-C₈-halogenoalkenyl comprising up to 9 halogen         atoms that can be the same or different; C₂-C₈-alkynyl;         C₂-C₈-halogenoalkynyl comprising up to 9 halogen atoms that can         be the same or different C₂-C₈-alkenyloxy;         C₂-C₈-halogenoalkenyloxy comprising up to 9 halogen atoms that         can be the same or different; C₂-C₈-alkynyloxy;         C₂-C₈-halogenoalkynyloxy comprising up to 9 halogen atoms that         can be the same or different; C₃-C₇-cycloalkyl;         C₃-C₇-cycloalkyl-C₁-C₈-alkyl; C₃-C₇-halogenocycloalkyl         comprising up to 9 halogen atoms that can be the same or         different; formyl; formyloxy; formylamino; carboxy; carbamoyl;         N-hydroxycarbamoyl; carbamate; (hydroxyimino)-C₁-C₈-alkyl;         C₁-C₈-alkylcarbonyl; C₁-C₈-halogenoalkylcarbonyl comprising up         to 9 halogen atoms that can be the same or different;         C₁-C₈-alkylcarbamoyl; di-C₁-C₈-alkylcarbamoyl; N—C₁-C₈-al         kyloxycarbamoyl; C₁-C₈-alkoxycarbarmoyl;         N—C₁-C₈-alkyl-C₁-C₈-alkoxycarbarmoyl; C₁-C₈-al koxycarbonyl;         C₁-C₈-halogenoalkoxycarbonyl comprising up to 9 halogen atoms         that can be the same or different; C₁-C₈-alkylaminocarbonyl;         di-C₁-C₈-alkylaminocarbonyl; C₁-C₈-alkylcarbonyloxy;         C₁-C₈-halogenoalkylcarbonyloxy comprising up to 9 halogen atoms         that can be the same or different; C₁-C₈-alkylcarbonylamino;         C₁-C₈-halogenoalkylcarbonylamino comprising up to 9 halogen         atoms that can be the same or different; C₁-C₈-al         kylaminocarbonyloxy; di-C₁-C₈-alkylam inocarbonyloxy;         C₁-C₈-alkyloxycarbonyloxy, C₁-C₈-alkylsulphenyl,         C₁-C₈-halogenoalkylsulphenyl comprising up to 9 halogen atoms         that can be the same or different, C₁-C₈-alkylsulphinyl,         C₁-C₈-halogenoalkylsulphinyl comprising up to 9 halogen atoms         that can be the same or different, C₁-C₈-alkylsulphonyl,         C₁-C₈-halogenoalkylsulphonyl comprising up to 9 halogen atoms         that can be the same or different, C₁-C₈-alkoxyimino,         (C₁-C₈-alkoxyimino)-C₁-C₈-alkyl,         (C₁-C₈-alkenyloxyimino)-C₁-C₈-alkyl,         (C₁-C₈-alkynyloxyimino)-C₁-C₈-alkyl, a         (benzyloxyimino)-C₁-C₈-alkyl; tri(C₁-C₈-alkyl)silyl;         tri(C₁-C₈-alkyl)silyl-C₁-C₈-alkyl; phenyl that can be         substituted by up to 5 groups Q; benzyloxy that can be         substituted by up to 5 groups Q; benzylthio that can be         substituted by up to 5 groups Q; benzylamino that can be         substituted by up to 5 groups Q; naphtyl that can be substituted         by up to 6 groups Q; phenoxy that can be substituted by up to 5         groups Q; phenylamino that can be substituted by up to 5 groups         Q; phenylthio that can be substituted by up to 5 groups Q;         phenylmethylene that can be substituted by up to 5 groups Q;         pyridinyl that can be substituted by up to four groups Q and         pyridinyloxy that can be substituted by up to four groups Q;         phenoxymethylene that can be substituted by up to 5 groups Q;     -   two substituents Z³ or Z⁷ together with the consecutive carbon         atoms to that they are linked can form a 5- or 6-membered,         saturated or non-saturated, carbo- or hetero-cycle, that can be         substituted by up to four groups Q that can be the same or         different;     -   p represents 1, 2, or 3;     -   R, that can be the same or different, represent hydrogen atom;         halogen atom; cyano; nitro; amino; thio; pentafluoro-λ-6-thio;         C₁-C₈-alkylamino; di-C₁-C₈-alkylamino; tri(C₁-C₈-alkyl)silyl;         C₁-C₈-alkylsulphanyl; C₁-C₈-halogenoalkylsulphanyl comprising up         to 9 halogen atoms that can be the same or different;         C₁-C₈-alkyl; C₁-C₈-halogenoalkyl comprising up to 9 halogen         atoms that can be the same or different; C₂-C₈-alkenyl;         C₂-C₈-halogenoalkenyl comprising up to 9 halogen atoms that can         be the same or different; C₂-C₈-alkynyl; C₂-C₈-halogenoalkynyl         comprising up to 9 halogen atoms that can be the same or         different; C₁-C₈-alkoxy; C₁-C₈-halogenoalkoxy comprising up to 9         halogen atoms that can be the same or different;         C₂-C₈-alkenyloxy; C₂-C₈-alkynyloxy; C₃-C₇-cycloalkyl;         C₃-C₇-cycloalkyl-C₁-C₈-alkyl; C₁-C₈-alkylsulphinyl;         C₁-C₈-alkyl-sulphonyl; C₁-C₈alkoxyimino;         (C₁-C₈-alkoxyimino)-C₁-C₈-alkyl; (benzyloxyimino)-C₁-C₈-alkyl;         phenoxy; benzyloxy; benzylthio; benzylamino; naphtyl;         halogenophenoxy comprising up to 9 halogen atoms that can be the         same or different; C₁-C₈-alkylcarbonyl;         C₁-C₈-halogenoalkylcarbonyl comprising up to 9 halogen atoms         that can be the same or different; C₁-C₈-alkoxycarbonyl;         C₁-C₈-halogenoalkoxycarbonyl comprising up to 9 halogen atoms         that can be the same or different; C₁-C₈-alkylaminocarbonyl;         di-C₁-C₈-alkylaminocarbonyl;     -   R^(a) and R^(b), that can be the same or different, represent a         hydrogen atom; C₁-C₈-alkyl; C₁-C₈-halogenoalkyl comprising up to         9 halogen atoms that can be the same or different;         C₁-C₈-alkoxy-C₁-C₈-alkyl; C₂-C₈-alkenyl; C₂-C₈-halogenoalkenyl         comprising up to 9 halogen atoms that can be the same or         different; C₂-C₈-alkynyl; C₂-C₈-halogenoalkynyl comprising up to         9 halogen atoms that can be the same or different;         C₃-C₇-cycloalkyl; C₃-C₇-cycloalkyl-C₁-C₈-alkyl;         C₃-C₇-halogenocycloalkyl comprising up to 9 halogen atoms that         can be the same or different; formyl; C₁-C₈-alkylcarbonyl;         C₁-C₈-halogenoalkylcarbonyl comprising up to 9 halogen atoms         that can be the same or different; C₁-C₈-alkylsulphonyl;         C₁-C₈-halogenoalkylsulphonyl comprising up to 9 halogen atoms         that can be the same or different; phenyl that can be         substituted by up to 5 groups Q; naphthyl that can be         substituted by up to 6 groups Q; phenylmethylene that can be         substituted by up to 5 groups Q; phenylsulphonyl that can be         substituted by up to 5 groups Q;     -   Z⁴ and Z⁵, that can be the same or different, represent a         hydrogen atom; a halogen atoms; cyano; nitro, C₁-C₈-alkyl;         C₁-C₈-halogenoalkyl comprising up to 9 halogen atoms that can be         the same or different; C₁-C₈-alkoxy; C₁-C₈-halogenoalkoxy         comprising up to 9 halogen atoms that can be the same or         different; C₁-C₈-alkoxy-C₁-C₈-alkyl; C₂-C₈-alkenyl;         C₂-C₈-halogenoalkenyl comprising up to 9 halogen atoms that can         be the same or different; C₂-C₈-alkynyl; C₂-C₈-halogenoalkynyl         comprising up to 9 halogen atoms that can be the same or         different; C₃-C₇-cycloalkyl; C₃-C₇-cycloalkyl-C₁-C₈-alkyl;         C₃-C₇-halogenocycloalkyl comprising up to 9 halogen atoms that         can be the same or different; formyl; C₁-C₈-alkylcarbonyl;         C₁-C₈-halogenoalkylcarbonyl comprising up to 9 halogen atoms         that can be the same or different; C₁-C₈-alkylsulphanyl;         C₁-C₈-halogenoalkylsulphanyl comprising up to 9 halogen atoms         that can be the same or different; C₁-C₈-alkylsulphinyl;         C₁-C₈-halogenoalkylsulphinyl comprising up to 9 halogen atoms         that can be the same or different; C₁-C₈-alkylsulphonyl;         C₁-C₈-halogenoalkylsulphonyl comprising up to 9 halogen atoms         that can be the same or different;     -   Z⁶ represents a hydrogen atom; C₁-C₈-alkyl; C₁-C₈-halogenoalkyl         comprising up to 9 halogen atoms that can be the same or         different; C₁-C₈-alkoxy-C₁-C₈-alkyl; C₂-C₈-alkenyl;         C₂-C₈-halogenoalkenyl comprising up to 9 halogen atoms that can         be the same or different; C₂-C₈-alkynyl; C₂-C₈-halogenoalkynyl         comprising up to 9 halogen atoms that can be the same or         different; C₃-C₇-cycloalkyl; C₃-C₇-cycloalkyl-C₁-C₈-alkyl;         C₃-C₇-halogenocycloalkyl comprising up to 9 halogen atoms that         can be the same or different; formyl, C₁-C₈-alkylcarbonyl;         C₁-C₈-halogenoalkylcarbonyl comprising up to 9 halogen atoms         that can be the same or different; C₁-C₈-alkylsulphonyl;         C₁-C₈-halogenoalkylsulphonyl comprising up to 9 halogen atoms         that can be the same or different; phenylsulfonyl can be         substituted by up to 5 groups Q; benzyl that can be substituted         by up to 5 groups Q;     -   Q, that can be the same or different, represents a halogen atom;         cyano; nitro; C₁-C₈-alkyl; C₁-C₈-halogenoalkyl comprising up to         9 halogen atoms that can be the same or different; C₁-C₈-alkoxy;         C₁-C₈-halogenoalkoxy comprising up to 9 halogen atoms that can         be the same or different; C₁-C₈-alkylsulphanyl;         C₁-C₈-halogenoalkylsulphanyl comprising up to 9 halogen atoms         that can be the same or different; tri(C₁-C₈)alkylsilyl and         tri(C₁-C₈)alkylsilyl-C₁-C₈-alkyl;         as well as salts, N-oxides, metallic complexes, metalloidic         complexes and optically active or geometric isomers thereof.

Any of the compounds according to the invention can exist as one or more stereoisomers depending on the number of stereogenic units (as defined by the IUPAC rules) in the compound. The invention thus relates equally to all the stereoisomers, and to the mixtures of all the possible stereoisomers, in all proportions. The stereoisomers can be separated according to the methods that are known per se by the man ordinary skilled in the art.

According to the invention, the following generic terms are generally used with the following meanings:

-   -   halogen means fluorine, chlorine, bromine or iodine;     -   heteroatom can be nitrogen, oxygen or sulphur;     -   halogenated groups, notably haloalkyl, haloalkoxy and cycloalkyl         groups, can comprise up to nine identical or different a halogen         atoms;     -   Any alkyl, alkenyl or alkynyl group can be linear or branched;     -   the term “aryl” means phenyl or naphthyl, optionally substituted         by one to five groups selected in the list consisting of         halogen, [C₁-C₆]-alkyl, [C₁-C₆]-haloalkyl, [C₂-C₆]-alkenyl,         [C₂-C₆]-haloalkenyl, [C₂-C₆]-alkynyl, [C₂-C₆]-haloalkynyl,         [C₁-C₆]-alkoxy, [C₁-C₄]-alkoxy-[C₁-C₄]-alkyl,         [C₁-C₄]-alkoxy-[C₁-C₆]-alkoxy, [C₁-C₆]-haloalkoxy and         [C₁-C₄]-haloalkoxy-[C₁-C₄]-alkyl;     -   In the case of an amino group or the amino moiety of any other         amino-containing group, substituted by two substituents that can         be the same or different, the two substituents together with the         nitrogen atom to that they are linked can form a heterocyclyl         group, preferably a 5- to 7-membered heterocyclyl group, that         can be substituted or that can include other hetero atoms, for         example a morpholino group or piperidinyl.

Preferred compounds of formula (I) according to the invention are those wherein A is selected in the list consisting of:

-   -   a heterocycle of formula (A1)

wherein:

R¹ to R³ that can be the same or different represent a hydrogen atom; a halogen atom; alkyl; C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy or C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different;

-   -   a heterocycle of formula (A²)

wherein:

R⁴ to R⁶ that can be the same or different represent a hydrogen atom; a halogen atom; C₁-C₅-alkyl; C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy or C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different;

-   -   a heterocycle of formula (A³)

wherein:

R⁷ represents a hydrogen atom; a halogen atom; C₁-C₅-alkyl; C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy or C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different;

R⁸ represents a hydrogen atom or a C₁-C₅-alkyl;

-   -   a heterocycle of formula (A⁴)

wherein:

R⁹ to R¹¹ that can be the same or different represent a hydrogen atom; a halogen atom; C₁-C₅-alkyl; amino; C₁-C₅-alkoxy; C₁-C₅-alkylsulphanyl C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different or C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different;

-   -   a heterocycle of formula (A⁵)

-   -   wherein:

R¹² to R¹⁴ that can be the same or different represent a hydrogen atom; a halogen atom; C₁-C₅-alkyl; C₁-C₅-alkoxy; amino; C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different or C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different;

-   -   a heterocycle of formula (A⁶)

wherein:

R¹⁵ represents a hydrogen atom; a halogen atom; a cyano; C₁-C₅-alkyl; C₁-C₅-alkoxy; C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different or C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; R¹⁶ and R¹⁸ that can be the same or different represent a hydrogen atom; a halogen atom; C₁-C₅-alkoxycarbonyl;; C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different or C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different;

R¹⁷ represents a hydrogen atom or C₁-C₅-alkyl;

-   -   a heterocycle of formula (A⁷)

wherein:

R¹⁹ represents a hydrogen atom or a C₁-C₅-alkyl;

R²⁰ to R²² that can be the same or different represent a hydrogen atom; a halogen atom; C₁-C₅-alkyl or C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy; C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different;

-   -   a heterocycle of formula (A⁸)

wherein:

R²³ represents a hydrogen atom; a halogen atom; C₁-C₅-alkyl or C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy; C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different;

R²⁴ represents a hydrogen atom or C₁-C₅-alkyl or C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different;

-   -   a heterocycle of formula (A9)

wherein:

R²⁵ represents a hydrogen atom; a halogen atom; C₁-C₅-alkyl or C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy; C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different; R²⁶ represents a hydrogen atom; C₁-C₅-alkyl or C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different;

-   -   a heterocycle of formula (A¹⁰)

wherein:

R²⁷ represents a hydrogen atom; a halogen atom; C₁-C₅-alkyl or C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy; C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different;

R²⁸ represents a hydrogen atom; a halogen atom; amino; C₁-C₅-alkyl or C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy; C1-C5-halogenoalkoxy comprising up to 9 halogen atoms which can be the same or different; C₁-C₅-alkylsulfanyl or C₁-C₅-halogenoalkylsulfanyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkylamino or di(C₁-C₅-alkyl)amino;

-   -   a heterocycle of formula (A¹¹)

wherein:

R²⁹ represents a hydrogen atom; a halogen atom; C₁-C₅-alkyl; C₁-C₅-alkoxy; C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different or C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different;

R³⁹ represents a hydrogen atom; a halogen atom; C₁-C₅-alkyl; C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy; C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkylsulfanyl or C₁-C₅-halogenoalkylsulfanyl comprising up to 9 halogen atoms that can be the same or different; amino; C₁-C₅-alkylamino or di-C₁-C₅-alkylamino;

-   -   a heterocycle of formula (A¹²)

wherein:

R³¹ represents a hydrogen atom; a halogen atom or a C₁-C₅-alkyl;

R³² represents a hydrogen atom; a halogen atom; C₁-C₅-alkyl or C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different;

R³³ represents a hydrogen atom; a halogen atom; a nitro; C₁-C₅-alkyl; C₁-C₅-alkoxy; C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different or C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different;

-   -   a heterocycle of formula (A¹³)

wherein:

R³⁴ represents a hydrogen atom; a halogen atom; C₁-C₅-alkyl; C₃-C₅-cycloalkyl; C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy; C₂-C₅-alkynyloxy or C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different;

R³⁵ represents a hydrogen atom; a halogen atom; C₁-C₅-alkyl; a cyano; C₁-C₅-alkoxy; C₁-C₅-alkylsulphanyl; C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different; amino; C₁-C₅-alkylamino or di(C₁-C₅-alkyl)amino;

R³⁶ represents a hydrogen atom or C₁-C₅-alkyl;

-   -   a heterocycle of formula (A¹⁴)

wherein:

R³⁷ and R³⁸ that can be the same or different represent a hydrogen atom; a halogen atom; C₁-C₅-alkyl; C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms which can be the same or different; C₁-C₅-alkoxy; C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different;or a C₁-C₅-alkylsulfanyl;

R³⁹ represents a hydrogen atom or C₁-C₅-alkyl;

-   -   a heterocycle of formula (A¹⁵)

wherein:

R⁴⁰ and R⁴¹ that can be the same or different represent a hydrogen atom; a halogen atom; C₁-C₅-alkyl or C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy; C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different;

-   -   a heterocycle of formula (A¹⁶)

wherein:

R⁴² and R⁴³ that can be the same or different represent a hydrogen atom; a halogen atom; C₁-C₅-alkyl; C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy; C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different or amino;

-   -   a heterocycle of formula (A¹⁷)

wherein:

R⁴⁴ and R⁴⁵ that can be the same or different represent a hydrogen atom; a halogen atom; C₁-C₅-alkyl; C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms which can be the same or different; C₁-C₅-alkoxy or C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different;

-   -   a heterocycle of formula (A¹⁸)

wherein:

R⁴⁷ represents a hydrogen atom; a halogen atom; C₁-C₅-alkyl or C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy; C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different;

R⁴⁶ represents a hydrogen atom; a halogen atom; C₁-C₅-alkyl; C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy; C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different or C₁-C₅-alkylsulphanyl;

-   -   a heterocycle of formula (A¹⁹)

wherein:

R⁴⁸ and R⁴⁹ that can be the same or different represent a hydrogen atom; a halogen atom; C₁-C₅-alkyl; C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy; C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different or C₁-C₅-alkylsulphanyl;

-   -   a heterocycle of formula (A²⁰)

wherein:

R⁵⁰ and R⁵¹ that can be the same or different represent a hydrogen atom; a halogen atom; C₁-C₅-alkyl; C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy; C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different or C₁-C₅-alkylsulphanyl;

-   -   a heterocycle of formula (A²¹)

wherein:

R⁵² represents a hydrogen atom; a halogen atom; C₁-C₅-alkyl or C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy; C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different;

-   -   a heterocycle of formula (A²²)

wherein:

R⁵³ represents a hydrogen atom; a halogen atom; C₁-C₅-alkyl or C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy; C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different;

-   -   a heterocycle of formula (A²³)

wherein:

R⁵⁴ and R⁵⁵ that can be the same or different represent a hydrogen atom; a halogen atom; C₁-C₅-alkyl or C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy; C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different;

R⁵⁶ represents a hydrogen atom or C₁-C₅-alkyl;

-   -   a heterocycle of formula (A²⁴)

wherein:

R⁵⁷ and R⁵⁹ that can be the same or different represent a hydrogen atom; a halogen atom; C₁-C₅-alkyl or C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy; C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different;

R⁵⁸ represents a hydrogen atom or C₁-C₅-alkyl;

-   -   a heterocycle of formula (A²⁵)

wherein:

R⁶⁰ and R⁶¹ that can be the same or different represent a hydrogen atom; a halogen atom; C₁-C₅-alkyl or C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different;

R⁶² represents a hydrogen atom or C₁-C₅-alkyl;

-   -   a heterocycle of formula (A²⁶)

wherein:

R⁶³ represents a hydrogen atom; a halogen atom; C₁-C₅-alkyl; a cyano; C₁-C₅-alkoxy; C₁-C₅-alkylsulphanyl; C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different; amino; C₁-C₅-alkylamino or di(C₁-C₅-alkyl)amino;

R⁶⁴ represents a hydrogen atom or C₁-C₅-alkyl;

R⁶⁵ represents a hydrogen atom; a halogen atom; C₁-C₅-alkyl; C₃-C₅-cycloalkyl; C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₅-alkoxy; C₂-C₅-alkynyloxy or C₁-C₅-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different.

More preferred compounds of formula (I) according are those wherein A is selected in the list consisting of A²; A⁶, A¹⁰ and A¹³.

Even more preferred compounds according to the invention are those wherein A represents A¹³ wherein R³⁴ represents C₁-C₅-alkyl C₁-C₅-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; R³⁵ represents a hydrogen or a fluorine atom; R³⁶ represents methyl.

Other preferred compounds of formula (I) according to the invention are those wherein T represents O or S.

Other more preferred compounds according to the invention are those wherein T represents O.

Other preferred compounds of formula (I) according to the invention are those wherein Z¹ represents cyclopropyl.

Other more preferred compounds according to the invention are those wherein those wherein Z¹ represents a non-substituted cyclopropyl.

Other preferred compounds of formula (I) according to the invention are those wherein Z² represents a hydrogen atom.

Other preferred compounds of formula (I) according to the invention are those wherein L¹ represents CZ⁴Z⁵.

Other preferred compounds of formula (I) according to the invention are those wherein L² represents CZ⁴Z⁵ and m represents 1 or 2.

Other preferred compounds of formula (I) according to the invention are those wherein Z³ and Z⁷, that can be the same or different, represent a hydrogen atom; a halogen atom; C₁-C₈-alkyl; C₁-C₈-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkoxy or C₁-C₈-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different.

The above mentioned preferences with regard to the substituents of the compounds of formula (I) according to the invention can be combined in various manners, either individually, partially or entirely. These combinations of preferred features thus provide sub-classes of compounds according to the invention. Examples of such sub-classes of preferred compounds according to the invention can combine:

-   -   preferred features of A with preferred features of one or more         of T, Z¹, Z², L¹, L², m, Z³ and Z⁷;     -   preferred features of T with preferred features of one or more         of A, Z¹, Z², L¹, L², m, Z³ and Z⁷;     -   preferred features of Z¹ with preferred features of one or more         of A, T, Z², L¹, L², m, Z³ and Z⁷;     -   preferred features of Z² with preferred features of one or more         of A, T, Z¹, L¹, L², m, Z³ and Z⁷;     -   preferred features of L¹ with preferred features of one or more         of A, T, Z¹, Z², L², m, Z³ and Z⁷;     -   preferred features of L² with preferred features of one or more         of A, T, Z¹, Z², L¹, m, Z³ and Z⁷;     -   preferred features of m with preferred features of one or more         of A, T, Z¹, Z², L¹, L², Z³ and Z⁷;     -   preferred features of Z³ with preferred features of one or more         of A, T, Z¹, Z², L¹, L², m and Z⁷;     -   preferred features of Z⁷ with preferred features of one or more         of A, T, Z¹, Z², L¹, L², m and Z³.

In these combinations of preferred features of the substituents of the compounds according to the invention, the said preferred features can also be selected among the more preferred features of each of A, T, Z¹, Z², L¹, L², m, Z³ and Z⁷ so as to form most preferred subclasses of compounds according to the invention.

The present invention also relates to a process for the preparation of compounds of formula (I). Thus according to a further aspect of the present invention there is provided a process P1 for the preparation of a compound of formula (I) as herein-defined, as illustrated by the following reaction scheme:

wherein

-   -   T represents O, N—R^(a), N—OR^(a), N—NR^(a)R^(b) or N—CN;     -   Y¹ represents a halogen atom or a hydroxyl;     -   A, Z¹ to Z³, R^(a), R^(b), L¹, L², X, m and p are as         herein-defined

In process P1 according to the invention, step 1 can be performed if appropriate in the presence of a solvent and if appropriate in the presence of an acid binder.

N-cycloalkyl-amine derivatives of formula (II) are known or can be prepared by known processes (J. Het. Chem., 1983, p1031-6; J. Am. Chem. Soc., 2004, p 5192-5201; Synt. Comm. 2003, p 3419-25; Chem. Pharm. Bull, 1981, 29(3),720).

When T represents O, carboxylic acid derivatives of formula (III) are known or can be prepared by known processes (WO-93/11117; EP-A 0 545 099; Nucleosides & Nucleotides, 1987, p 737-759, Bioorg. Med. Chem., 2002, p 2105-2108).

When T represents N—R^(a), N—OR^(a), N—NR^(a)R^(b) or N—CN, N-substituted carboximidoyl chloride derivatives of formula (III) are known or can be prepared by known processes, for example as described in Houben-Weyl, “Methoden der organischen Chemie” (1985), E5/1, 628-633 and Patai, “The chemistry of amidines and imidates” (1975), 296-301.

Suitable acid binders for carrying out process P1 according to the invention can be inorganic or organic bases which are customary for such reactions. Preference is given to using alkaline earth metal or alkali metal hydroxides, such as sodium hydroxide, calcium hydroxide, potassium hydroxide or other ammonium hydroxide derivatives; alkali metal carbonates, such as sodium carbonate, potassium carbonate, potassium bicarbonate, sodium bicarbonate; alkali metal or alkaline earth metal acetates, such as sodium acetate, potassium acetate, calcium acetate; alkaline earth metal or alkali metal hydrides, such as sodium hydride or potassium hydride; alkaline earth metal or alkali metal alcoolates, such as sodium methylate, sodium ethylate, sodium propylate or potassium t-butylate;and also tertiary amines, such as trimethylamine, triethylamine, tributylamine, N,N-dimethylaniline, pyridine, N-methylpiperidine, N,N-dimethyl-aminopyridine, diazabicyclooctane (DABCO), diazabicyclononene (DBN) or diaza-bicycloundecene (DBU) or a polymer-supported acid scavenger (for example as detailed in http://www.iris-biotech.de/down loads/scavengers.pdf).

It is also possible to work in the absence of any additional acid binder or to employ an excess of the amine component, so that it simultaneously acts as acid binder agent.

Suitable solvents for carrying out process P1 according to the invention can be customary inert organic solvents. Preference is given to using optionally halogenated aliphatic, alicyclic or aromatic hydrocarbons, such as petroleum ether, hexane, heptane, cyclohexane, methylcyclohexane, benzene, toluene, xylene or decalin; chlorobenzene, dichlorobenzene, dichloromethane, chloroform, carbon tetrachloride, dichlorethane or trichlorethane; ethers, such as diethyl ether, diisopropyl ether, methyl t-butyl ether, methyl t-amyl ether, dioxane, tetrahydrofuran, 1,2-dimethoxyethane, 1,2-diethoxyethane or anisole; nitriles, such as acetonitrile, propionitrile, n- or i-butyronitrile or benzonitrile; amides, such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methylformanilide, N-methylpyrrolidone, or hexamethylphosphoric triamide; alcohols such as methanol, ethanol, propanol, iso-propanol; esters, such as methyl acetate or ethyl acetate, sulphoxides, such as dimethyl sulphoxide, or sulphones, such as sulpholane.

When carrying out process P1 according to the invention, the amine derivative of formula (II) can be employed as its salt, such as chlorhydate or any other convenient salt.

When carrying out process P1 according to the invention, 1 mole or an excess of the amine derivative of formula (II) and from 1 to 3 moles of the acid binder can be employed per mole of the reagent of formula (III).

It is also possible to employ the reaction components in other ratios. Work-up is carried out by known methods.

In general, the reaction mixture is concentrated under reduced pressure. The residue that remains can be freed by known methods, such as chromatography or recrystallization, from any impurities that can still be present.

According to a further aspect according to the invention, there is provided a process P2 for the preparation of a compound of formula (I) wherein T represents S, as herein-defined, as illustrated by the following reaction scheme :

wherein A, Z¹ to Z³, L¹, L², X, m, p and Y are as herein-defined;

Process P2 can be performed in the presence of a thionating agent.

Starting amide derivatives of formula (I) can be prepared according to process P1 wherein T represents O.

Suitable thionating agents for carrying out process P2 according to the invention can be sulphur (S), sulfhydric acid (H₂S), sodium sulfide (Na₂S), sodium hydrosulfide (NaHS), boron trisulfide (B₂S₃), bis (diethylaluminium) sulfide ((AlEt₂)₂S), ammonium sulfide ((NH₄)₂S), phosphorous pentasulfide (P₂S₅), Lawesson's reagent (2,4-bis(4-methoxyphenyl)-1,2,3,4-dithiadiphosphetane 2,4-disulfide) or a polymer-supported thionating reagent such as described in J. Chem. Soc. Perkin 1, (2001), 358. in the presence or not of a catalytic, stoechiometric or more amount of a base such as an inorganic or organic base. Preference is given to using alkali metal carbonates, such as sodium carbonate, potassium carbonate, potassium bicarbonate, sodium bicarbonate; heterocyclic aromatic bases, such as pyridine, picoline, lutidine, collidine; and also tertiary amines, such as trimethylamine, triethylamine, tributylamine, N,N-dimethylaniline, N,N-dimethyl-aminopyridine or N-methylpiperidine.

Suitable solvents for carrying out process P2 according to the invention can be customary inert organic solvents. Preference is given to using optionally halogenated aliphatic, alicyclic or aromatic hydrocarbons, such as petroleum ether, hexane, heptane, cyclohexane, methylcyclohexane, benzene, toluene, xylene or decalin; chlorobenzene, dichlorobenzene, dichloromethane, chloroform, carbon tetrachloride, dichlorethane or trichlorethane; ethers, such as diethyl ether, diisopropyl ether, methyl t-butyl ether, methyl t-amyl ether, dioxane, tetrahydrofuran, 1,2-dimethoxyethane or 1,2-diethoxyethane; nitriles, such as acetonitrile, propionitrile, n- or i-butyronitrile or benzonitrile; sulphurous solvents, such as sulpholane or carbon disufide.

When carrying out process P2 according to the invention, 1 mole or an excess of the sulphur equivalent of the thionating agent and from 1 to 3 moles of the base can be employed per mole of the amide reactant (I).

It is also possible to employ the reaction components in other ratios. Work-up is carried out by known methods.

In general, the reaction mixture is concentrated under reduced pressure. The residue that remains can be freed by known methods, such as chromatography or recrystallization, from any impurities that can still be present.

When carrying out processes P1 and P2 according to the invention, the reaction temperatures can be varied within a relatively wide range. In general, these processes are carried out at temperatures from 0° C. to 160° C., preferably from 10° C. to 120° C. A way to control the temperature for the processes according to the invention is to use micro-wave technology.

Processes P1 and P2 according to the invention are generally carried out under atmospheric pressure. It is also possible to operate under elevated or reduced pressure.

Compounds according to the invention can be prepared according to the above described processes. It will nevertheless be understood that, on the basis of his general knowledge and of available publications, the skilled worker will be able to adapt these processes according to the specifics of each of the compounds according to the invention that is desired to be synthesized.

Still in a further aspect, the present invention relates to compounds of formula (II) useful as intermediate compounds or materials for the process of preparation according to the invention. The present invention thus provides compounds of formula (II)

wherein Z¹, Z², L¹, L², m, X, Z³ and p are as herein-defined provided that X represents N when Z⁴ and Z⁵ both represent a hydrogen atom or when L² represents NZ⁶ and that compound of formula (II) is not 3-(cyclopropylamino)-2,3-dihydro-1,7-dimethyl-1H-indan-4-ol.

In a further aspect, the present invention also relates to a fungicide composition comprising an effective and non-phytotoxic amount of an active compound of formula (I).

The expression “effective and non-phytotoxic amount” means an amount of composition according to the invention that is sufficient to control or destroy the fungi present or liable to appear on the crops, and that does not entail any appreciable symptom of phytotoxicity for the said crops. Such an amount can vary within a wide range depending on the fungus to be controlled, the type of crop, the climatic conditions and the compounds included in the fungicide composition according to the invention. This amount can be determined by systematic field trials that are within the capabilities of a person skilled in the art.

Thus, according to the invention, there is provided a fungicide composition comprising, as an active ingredient, an effective amount of a compound of formula (I) as herein defined and an agriculturally acceptable support, carrier or filler.

According to the invention, the term “support” denotes a natural or synthetic, organic or inorganic compound with that the active compound of formula (I) is combined or associated to make it easier to apply, notably to the parts of the plant. This support is thus generally inert and should be agriculturally acceptable. The support can be a solid or a liquid. Examples of suitable supports include clays, natural or synthetic silicates, silica, resins, waxes, solid fertilisers, water, alcohols, in particular butanol, organic solvents, mineral and plant oils and derivatives thereof. Mixtures of such supports can also be used.

The composition according to the invention can also comprise additional components. In particular, the composition can further comprise a surfactant. The surfactant can be an emulsifier, a dispersing agent or a wetting agent of ionic or non-ionic type or a mixture of such surfactants. Mention can be made, for example, of polyacrylic acid salts, lignosulphonic acid salts, phenolsulphonic or naphthalenesulphonic acid salts, polycondensates of ethylene oxide with fatty alcohols or with fatty acids or with fatty amines, substituted phenols (in particular alkylphenols or arylphenols), salts of sulphosuccinic acid esters, taurine derivatives (in particular alkyl taurates), phosphoric esters of polyoxyethylated alcohols or phenols, fatty acid esters of polyols, and derivatives of the above compounds containing sulphate, sulphonate and phosphate functions. The presence of at least one surfactant is generally essential when the active compound and/or the inert support are water-insoluble and when the vector agent for the application is water. Preferably, surfactant content can be comprised from 5% to 40% by weight of the composition.

Optionally, additional components can also be included, e.g. protective colloids, adhesives, thickeners, thixotropic agents, penetration agents, stabilisers, sequestering agents. More generally, the active compounds can be combined with any solid or liquid additive that complies with the usual formulation techniques.

In general, the composition according to the invention can contain from 0.05 to 99% by weight of active compound, preferably 10 to 70% by weight.

Compositions according to the invention can be used in various forms such as aerosol dispenser, capsule suspension, cold fogging concentrate, dustable powder, emulsifiable concentrate, emulsion oil in water, emulsion water in oil, encapsulated granule, fine granule, flowable concentrate for seed treatment, gas (under pressure),gas generating product, granule, hot fogging concentrate, macrogranule, microgranule, oil dispersible powder, oil miscible flowable concentrate, oil miscible liquid, paste, plant rodlet, powder for dry seed treatment, seed coated with a pesticide, soluble concentrate, soluble powder, solution for seed treatment, suspension concentrate (flowable concentrate), ultra low volume (ULV) liquid, ultra low volume (ULV) suspension, water dispersible granules or tablets, water dispersible powder for slurry treatment, water soluble granules or tablets, water soluble powder for seed treatment and wettable powder. These compositions include not only compositions that are ready to be applied to the plant or seed to be treated by means of a suitable device, such as a spraying or dusting device, but also concentrated commercial compositions that must be diluted before application to the crop.

The compounds according to the invention can also be mixed with one or more insecticide, fungicide, bactericide, attractant, acaricide or pheromone active substance or other compounds with biological activity. The mixtures thus obtained have normally a broadened spectrum of activity. The mixtures with other fungicide compounds are particularly advantageous.

Examples of suitable fungicide mixing partners can be selected in the following lists:

(1) Inhibitors of the nucleic acid synthesis, for example benalaxyl, benalaxyl-M, bupirimate, clozylacon, dimethirimol, ethirimol, furalaxyl, hymexazol, metalaxyl, metalaxyl-M, ofurace, oxadixyl and oxolinic acid.

(2) Inhibitors of the mitosis and cell division, for example benomyl, carbendazim, chlorfenazole, diethofencarb, ethaboxam, fuberidazole, pencycuron, thiabendazole, thiophanate, thiophanate-methyl and zoxamide.

(3) Inhibitors of the respiration, for example diflumetorim as Cl-respiration inhibitor; bixafen, boscalid, carboxin, fenfuram, flutolanil, fluopyram, furametpyr, furmecyclox, isopyrazam (9R-component), isopyrazam (9S-component), mepronil, oxycarboxin, penthiopyrad, thifluzamide as CII-respiration inhibitor; amisulbrom, azoxystrobin, cyazofamid, dimoxystrobin, enestroburin, famoxadone, fenamidone, fluoxastrobin, kresoxim-methyl, metominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, pyribencarb, trifloxystrobin as CIII-respiration inhibitor.

(4) Compounds capable to act as an uncoupler, like for example binapacryl, dinocap, fluazinam and meptyldinocap.

(5) Inhibitors of the ATP production, for example fentin acetate, fentin chloride, fentin hydroxide, and silthiofam.

(6) Inhibitors of the amino acid and/or protein biosynthesis, for example andoprim, blasticidin-S, cyprodinil, kasugamycin, kasugamycin hydrochloride hydrate, mepanipyrim and pyrimethanil.

(7) Inhibitors of the signal transduction, for example fenpiclonil, fludioxonil and quinoxyfen.

(8) Inhibitors of the lipid and membrane synthesis, for example biphenyl, chlozolinate, edifenphos, etridiazole, iodocarb, iprobenfos, iprodione, isoprothiolane, procymidone, propamocarb, propamocarb hydrochloride, pyrazophos, tolclofos-methyl and vinclozolin.

(9) Inhibitors of the ergosterol biosynthesis, for example aldimorph, azaconazole, bitertanol, bromuconazole, cyproconazole, diclobutrazole, difenoconazole, diniconazole, diniconazole-M, dodemorph, dodemorph acetate, epoxiconazole, etaconazole, fenarimol, fenbuconazole, fenhexamid, fenpropidin, fenpropimorph, fluquinconazole, flurprimidol, flusilazole, flutriafol, furconazole, furconazole-cis, hexaconazole, imazalil, imazalil sulfate, imibenconazole, ipconazole, metconazole, myclobutanil, naftifine, nuarimol, oxpoconazole, paclobutrazol, pefurazoate, penconazole, piperalin, prochloraz, propiconazole, prothioconazole, pyributicarb, pyrifenox, quinconazole, simeconazole, spiroxamine, tebuconazole, terbinafine, tetraconazole, triadimefon, triad imenol, tridemorph, triflumizole, triforine, triticonazole, uniconazole, viniconazole and voriconazole.

(10) Inhibitors of the cell wall synthesis, for example benthiavalicarb, dimethomorph, flumorph, iprovalicarb, mandipropamid, polyoxins, polyoxorim, prothiocarb, validamycin A, and valiphenal.

(11) Inhibitors of the melanine biosynthesis, for example carpropamid, diclocymet, fenoxanil, phthalide, pyroquilon and tricyclazole.

(12) Compounds capable to induce a host defence, like for example acibenzolar-S-methyl, probenazole, and tiadinil.

(13) Compounds capable to have a multisite action, like for example bordeaux mixture, captafol, captan, chlorothalonil, copper naphthenate, copper oxide, copper oxychloride, copper preparations such as copper hydroxide, copper sulphate, dichlofluanid, dithianon, dodine, dodine free base, ferbam, fluorofolpet, folpet, guazatine, guazatine acetate, iminoctadine, iminoctadine albesilate, iminoctadine triacetate, mancopper, mancozeb, maneb, metiram, metiram zinc, oxine-copper, propamidine, propineb, sulphur and sulphur preparations including calcium polysulphide, thiram, tolylfluanid, zineb and ziram.

(14) Further compounds like for example 2 ,3-dibutyl-6-chlorothieno[2,3-d]pyrimidin-4(3H)-one, ethyl (2Z)-3-amino-2-cyano-3-phenylprop-2-enoate, N-[2-(1,3-dimethylbutyl)phenyl]-5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide, N-{2-[1,1′-bi(cyclopropyl)-2-yl]phenyl}-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide, (2E)-2-(2-{[6-(3-chloro-2-methylphenoxy)-5-fluoropyrimidin-4-yl]oxy}phenyl)-2-(methoxyimino)-N-methylethanamide, (2E)-2-{2-[({[(2E,3E)-4-(2,6-dichlorophenyl)but-3-en-2-ylidene]amino}oxy)methyl]phenyl}-2-(methoxyimino)-N-methylethanamide, 2-chloro-N-(1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)pyridine-3-carboxamide, N-(3-ethyl-3,5,5-trimethylcyclohexyl)-3-(formylamino)-2-hydroxybenzamide, 5-methoxy-2-methyl-4-(2-{[({(1E)-1-[3-(trifluoromethyl)phenyl]ethylidene}amino)oxy]methyl}phenyl)-2,4-dihydro-3H-1,2,4-triazol-3-one, (2E)-2-(methoxyimino)-N-methyl-2-(2-{[({(1E)-1-[3-(trifluoromethyl)phenyl]ethylidene}amino)oxy]methyl}phenyl)ethanamide, (2E)-2-(methoxyimino)-N-methyl-2-{2-[(E)-({1-[3-(trifluoromethyl)phenyl]ethoxy}imino)methyl]phenyl}ethanamide, (2E)-2-{2-[({[(1E)-1-(3-{[(E)-1-fluoro-2-phenylethenyl]oxy}phenyl)ethylidene]amino}oxy)methyl]phenyl}-2-(methoxyimino)-N-methylethanamide, 1-(4-chlorophenyl)-2-(1H-1,2,4-triazol-1-yl)cycloheptanol, methyl 1-(2,2-dimethyl-2,3-dihydro-1H-inden-1-yl)-1H-imidazole-5-carboxylate, N-ethyl-N-methyl-N′-{2-methyl-5-(trifluoromethyl)-4-[3-(trimethylsilyl)propoxy]phenyl}imidoformamide, N′-{5-(difluoromethyl)-2-methyl-4-[3-(trimethylsilyl)propoxy]phenyl}-N-ethyl-N-methylimidoformamide, O-{1-[(4-methoxyphenoxy)methyl]-2,2-dimethylpropyl} 1H-imidazole-1-carbothioate, N-[2-(4-{[3-(4-chlorophenyl)prop-2-yn-1-yl]oxy}-3-methoxyphenyl)ethyl]-N2-(methylsulfonyl)valinamide, 5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)[1,2,4]triazolo[1,5-a]pyrimidine, 5-amino-1,3,4-thiadiazole-2-thiol, propamocarb-fosetyl, 1-[(4-methoxyphenoxy)methyl]-2,2-dimethylpropyl 1H-imidazole-1-carboxylate, 1-methyl-N-[2-(1,1,2,2-tetrafluoroethoxy)phenyl]-3-(trifluoromethyl)-1H-pyrazole-4-carboxamide, 2,3,5,6-tetrachloro-4-(methylsulfonyl)pyridine, 2-butoxy-6-iodo-3-propyl-4H-chromen-4-one, 2-phenylphenol and salts, 3-(difluoromethyl)-1-methyl-N-[2-(1,1,2,2-tetrafluoroethoxy)phenyl]-1H-pyrazole-4-carboxamide, 3,4,5-trichloropyridine-2,6-dicarbonitrile, 3-[5-(4-chlorophenyl)-2,3-dimethylisoxazolidin-3-yl]pyridine, 3-chloro-5-(4-chlorophenyl)-4-(2,6-difluorophenyl)-6-methylpyridazine, 4-(4-chlorophenyl)-5-(2,6-difluorophenyl)-3,6-dimethylpyridazine, quinolin-8-ol, quinolin-8-ol sulfate (2:1) (salt), benthiazole, bethoxazin, capsimycin, carvone, chinomethionat, chloroneb, cufraneb, cyflufenamid, cymoxanil, cyprosulfamide, dazomet, debacarb, dichlorophen, diclomezine, dicloran, difenzoquat, difenzoquat methylsulphate, diphenylamine, ecomate, ferimzone, flumetover, fluopicolide, fluoroimide, flusulfamide, fosetyl-aluminium, fosetyl-calcium, fosetyl-sodium, hexachlorobenzene, irumamycin, isotianil, methasulfocarb, methyl (2E)-2-{2-[({cyclopropyl[(4-methoxyphenyl)imino]methyl)thio)methyl]phenyl}-3-methoxyacrylate, methyl isothiocyanate, metrafenone, (5-bromo-2-methoxy-4-methylpyridin-3-yl)(2,3,4-trimethoxy-6-methylphenyl)methanone, mildiomycin, tolnifanide, N-(4-chlorobenzyl)-3-[3-methoxy-4-(prop-2-yn-1-yloxy)phenyl]propanamide, N-[(4-chlorophenyl)(cyano)methyl]-3-[3-methoxy-4-(prop-2-yn-1-yloxy)phenyl]propanamide, N-[(5-bromo-3-chloropyridin-2-yl)methyl]-2,4-dichloropyridine-3-carboxamide, N-[1-(5-bromo-3-chloropyridin-2-ypethyl]-2,4-dichloropyridine-3-carboxamide, N-[1-(5-bromo-3-chloropyridin-2-yl)ethyl]-2-fluoro-4-iodopyridine-3-carboxamide, N-{(Z)-[(cyclopropylmethoxy)imino][6-(difluoromethoxy)-2,3-difluorophenyl]methyl}-2-phenylacetamide, N-{(E)-[(cyclopropylmethoxy)imino][6-(difluoromethoxy)-2,3-difluorophenyl]methyl}-2-phenylacetamide, natamycin, nickel dimethyldithiocarbamate, nitrothal-isopropyl, octhilinone, oxamocarb, oxyfenthiin, pentachlorophenol and salts, phenazine-l-carboxylic acid, phenothrin, phosphorous acid and its salts, propamocarb fosetylate, propanosine-sodium, proquinazid, pyrrolnitrine, quintozene, S-prop-2-en-1-yl 5-amino-2-(1-methylethyl)-4-(2-methylphenyl)-3-oxo-2,3-dihydro-1H-pyrazole-l-carbothioate, tecloftalam, tecnazene, triazoxide, trichlamide, 5-chloro-N′-phenyl-N′-prop-2-yn-l-ylthiophene-2-sulfonohydrazide and zarilamid.

The composition according to the invention comprising a mixture of a compound of formula (I) with a bactericide compound can also be particularly advantageous. Examples of suitable bactericide mixing partners can be selected in the following list: bronopol, dichlorophen, nitrapyrin, nickel dimethyldithiocarbamate, kasugamycin, octhilinone, furancarboxylic acid, oxytetracycline, probenazole, streptomycin, tecloftalam, copper sulphate and other copper preparations.

The compounds of formula (I) and the fungicide composition according to the invention can be used to curatively or preventively control the phytopathogenic fungi of plants or crops.

Thus, according to a further aspect of the invention, there is provided a method for curatively or preventively controlling the phytopathogenic fungi of plants or crops characterised in that a compound of formula (I) or a fungicide composition according to the invention is applied to the seed, the plant or to the fruit of the plant or to the soil wherein the plant is growing or wherein it is desired to grow.

The method of treatment according to the invention can also be useful to treat propagation material such as tubers or rhizomes, but also seeds, seedlings or seedlings pricking out and plants or plants pricking out. This method of treatment can also be useful to treat roots. The method of treatment according to the invention can also be useful to treat the overground parts of the plant such as trunks, stems or stalks, leaves, flowers and fruit of the concerned plant.

Among the plants that may becan be protected by the method according to the invention, mention may becan be made of cotton; flax; vine; fruit or vegetable crops such as Rosaceae sp. (for instance pip fruit such as apples and pears, but also stone fruit such as apricots, almonds and peaches), Ribesioidae sp., Juglandaceae sp., Betulaceae sp., Anacardiaceae sp., Fagaceae sp., Moraceae sp., Oleaceae sp., Actinidaceae sp., Lauraceae sp., Musaceae sp. (for instance banana trees and plantins), Rubiaceae sp., Theaceae sp., Sterculiceae sp., Rutaceae sp. (for instance lemons oranges and grapefruit); Solanaceae sp. (for instance tomatoes), Liliaceae sp., Asteraceae sp. (for instance lettuces), Umbelliferae sp., Cruciferae sp., Chenopodiaceae sp., Cucurbitaceae sp., Papilionaceae sp. (for instance peas), Rosaceae sp. (for instance strawberries); major crops such as Graminae sp. (for instance maize, lawn or cereals such as wheat, rye, rice, barley and triticale), Asteraceae sp. (for instance sunflower), Cruciferae sp. (for instance colza), Fabacae sp. (for instance peanuts), Papilionaceae sp. (for instance soybean), Solanaceae sp. (for instance potatoes), Chenopodiaceae sp. (for instance beetroots), Elaeis sp. (for instance oil palm); horticultural and forest crops; as well as genetically modified homologues of these crops.

Among the diseases of plants or crops that can be controlled by the method according to the invention, mention can be made of:

-   -   Powdery Mildew Diseases such as

Blumeria diseases caused for example by Blumeria graminis;

Podosphaera diseases caused for example by Podosphaera leucotricha;

Sphaerotheca diseases caused for example by Sphaerotheca fuliginea;

Uncinula diseases caused for example by Uncinula necator;

-   -   Rust Diseases such as

Gymnosporangium diseases caused for example by Gymnosporangium sabinae;

Hemileia diseases caused for example by Hemileia vastatrix;

Phakopsora diseases caused for example by Phakopsora pachyrhizi and Phakopsora meibomiae;

Puccinia diseases caused for example by Puccinia recondite, Puccinia graminis or Puccinia striiformis;

Uromyces diseases caused for example by Uromyces appendiculatus;

-   -   Oomycete Diseases such as

Albugo diseases caused for example by Albugo candida;

Bremia diseases caused for example by Bremia lactucae;

Peronospora diseases caused for example by Peronospora pisi and Peronospora brassicae;

Phytophthora diseases caused for example by Phytophthora infestans;

Plasmopara diseases caused for example by Plasmopara viticola;

Pseudoperonospora diseases caused for example by Pseudoperonospora humuli and Pseudoperonospora cubensis;

Pythium diseases caused for example by Pythium ultimum;

-   -   Leaf spot, Leaf blotch and Leaf Blight Diseases such as

Alternaria diseases caused for example by Alternaria solani;

Cercospora diseases caused for example by Cercospora beticola;

Cladiosporium diseases caused for example by Cladiosporium cucumerinum;

Cochliobolus diseases caused for example by Cochliobolus sativus (Conidiaform: Drechslera, Syn: Helminthosporium) or Cochliobolus miyabeanus;

Colletotrichum diseases caused for example by Colletotrichum lindemuthianum;

Cycloconium diseases caused for example by Cycloconium oleaginum;

Diaporthe diseases caused for example by Diaporthe citri;

Elsinoe diseases caused for example by Elsinoe fawcettii;

Gloeosporium diseases caused for example by Gloeosporium laeticolor;

Glomerella diseases caused for example by Glomerella cingulata;

Guignardia diseases caused for example by Guignardia bidwellii;

Leptosphaeria diseases caused for example by Leptosphaeria maculans and Leptosphaeria nodorum;

Magnaporthe diseases caused for example by Magnaporthe grisea;

Mycosphaerella diseases caused for example by Mycosphaerella graminicola, Mycosphaerella arachidicola and Mycosphaerella fijiensis;

Phaeosphaeria diseases caused for example by Phaeosphaeria nodorum;

Pyrenophora diseases caused for example by Pyrenophora teres or Pyrenophora tritici repentis;

Ramularia-diseases caused for example by Ramularia collo-cygni or Ramularia areola;

Rhynchosporium diseases caused for example by Rhynchosporium secalis;

Septoria diseases caused for example by Septoria apii and Septoria lycopersici;

Typhula diseases caused for example by Thyphula incarnate;

Venturia diseases caused for example by Venturia inaequalis;

-   -   Root-, Sheath and Stem Diseases such as

Corticium diseases caused for example by Corticium graminearum;

Fusarium diseases caused for example by Fusarium oxysporum;

Gaeumannomyces diseases caused for example by Gaeumannomyces graminis;

Rhizoctonia diseases caused for example by Rhizoctonia solani;

Sarocladium diseases caused for example by Sarocladium oryzae;

Sclerotium diseases caused for example by Sclerotium oryzae;

Tapesia diseases caused for example by Tapesia acuformis;

Thielaviopsis diseases caused for example by Thielaviopsis basicola;

-   -   Ear and Panicle Diseases including Maize cob such as

Alternaria diseases caused for example by Alternaria spp.;

Aspergillus diseases caused for example by Aspergillus flavus;

Cladosporium diseases caused for example by Cladiosporium cladosporioides;

Claviceps diseases caused for example by Claviceps purpurea;

Fusarium diseases caused for example by Fusarium culmorum;

Gibberella diseases caused for example by Gibberella zeae;

Monographella diseases caused for example by Monographella nivalis;

-   -   Smut- and Bunt Diseases such as

Sphacelotheca diseases caused for example by Sphacelotheca reiliana;

Tilletia diseases caused for example by Tilletia caries;

Urocystis diseases caused for example by Urocystis occulta;

Ustilago diseases caused for example by Ustilago nuda;

-   -   Fruit Rot and Mould Diseases such as

Aspergillus diseases caused for example by Aspergillus flavus;

Botrytis diseases caused for example by Botrytis cinerea;

Penicillium diseases caused for example by Penicillium expansum and Penicillium purpurogenum;

Rhizopus diseases caused by example by Rhizopus stolonifer

Sclerotinia diseases caused for example by Sclerotinia sclerotiorum;

Verticillium diseases caused for example by Verticillium alboatrum;

-   -   Seed- and Soilborne Decay, Mould, Wilt, Rot and Damping-off         diseases

Alternaria diseases caused for example by Alternaria brassicicola;

Aphanomyces diseases caused for example by Aphanomyces euteiches;

Ascochyta diseases caused for example by Ascochyta lentis;

Aspergillus diseases caused for example by Aspergillus flavus;

Cladosporium diseases caused for example by Cladosporium herbarum;

Cochliobolus diseases caused for example by Cochliobolus sativus;

(Conidiaform: Drechslera, Bipolaris Syn: Helminthosporium);

Colletotrichum diseases caused for example by Colletotrichum coccodes;

Fusarium diseases caused for example by Fusarium culmorum;

Gibberella diseases caused for example by Gibberella zeae;

Macrophomina diseases caused for example by Macrophomina phaseolina;

Microdochium diseases caused for example by Microdochium nivale;

Monographella diseases caused for example by Monographella nivalis;

Penicillium diseases caused for example by Penicillium expansum;

Phoma diseases caused for example by Phoma lingam;

Phomopsis diseases caused for example by Phomopsis sojae;

Phytophthora diseases caused for example by Phytophthora cactorum;

Pyrenophora diseases caused for example by Pyrenophora graminea;

Pyricularia diseases caused for example by Pyricularia oryzae;

Pythium diseases caused for example by Pythium ultimum;

Rhizoctonia diseases caused for example by Rhizoctonia solani;

Rhizopus diseases caused for example by Rhizopus oryzae;

Sclerotium diseases caused for example by Sclerotium rolfsii;

Septoria diseases caused for example by Septoria nodorum;

Typhula diseases caused for example by Typhula incarnate;

Verticillium diseases caused for example by Verticillium dahliae;

-   -   Canker, Broom and Dieback Diseases such as

Nectria diseases caused for example by Nectria galligena;

-   -   Blight Diseases such as

Monilinia diseases caused for example by Monilinia laxe;

-   -   Leaf Blister or Leaf Curl Diseases including deformation of         blooms and fruits such as

Exobasidium diseases caused for nexample by Exobasidium vexans.

Taphrina diseases caused for example by Taphrina deformans;

-   -   Decline Diseases of Wooden Plants such as

Esca disease caused for example by Phaeomoniella clamydospora, Phaeoacremonium aleophilum and Fomitiporia mediterranea;

Ganoderma diseases caused by example by Ganoderma boninense;

-   -   Diseases of Flowers and Seeds such as

Botrytis diseases caused for example by Botrytis cinerea; ‘Diseases of Tubers such as

Rhizoctonia diseases caused for example by Rhizoctonia solani;

Helminthosporium diseases caused for example by Helminthosporium solani;

-   -   Club root diseases such as

Plasmodiophora diseases, cause for example by Plamodiophora brassicae.

-   -   Diseases caused by Bacterial Organisms such as

Xanthomanas species for example Xanthomonas campestris pv. oryzae;

Pseudomonas species for example Pseudomonas syringae pv. lachrymans;

Erwinia species for example Erwinia amylovora.

The fungicide composition according to the invention can also be used against fungal diseases liable to grow on or inside timber. The term “timber” means all types of species of wood, and all types of working of this wood intended for construction, for example solid wood, high-density wood, laminated wood, and plywood. The method for treating timber according to the invention mainly consists in contacting one or more compounds according to the invention, or a composition according to the invention; this includes for example direct application, spraying, dipping, injection or any other suitable means.

The dose of active compound usually applied in the method of treatment according to the invention is generally and advantageously from 10 to 800 g/ha, preferably from 50 to 300 g/ha for applications in foliar treatment. The dose of active substance applied is generally and advantageously from 2 to 200 g per 100 kg of seed, preferably from 3 to 150 g per 100 kg of seed in the case of seed treatment.

It is clearly understood that the doses indicated herein are given as illustrative examples of the method according to the invention. A person skilled in the art will know how to adapt the application doses, notably according to the nature of the plant or crop to be treated.

The fungicide composition according to the invention can also be used in the treatment of genetically modified organisms with the compounds according to the invention or the agrochemical compositions according to the invention. Genetically modified plants are plants into genome of that a heterologous gene encoding a protein of interest has been stably integrated. The expression “heterologous gene encoding a protein of interest” essentially means genes that give the transformed plant new agronomic properties, or genes for improving the agronomic quality of the modified plant.

The compounds or mixtures according to the invention can also be used for the preparation of composition useful to curatively or preventively treat human or animal fungal diseases such as, for example, mycoses, dermatoses, trichophyton diseases and candidiases or diseases caused by Aspergillus spp., for example Aspergillus fumigatus.

The various aspects of the invention will now be illustrated with reference to the following table of active or intermediate compound examples and the following preparation or efficacy examples. The following tables illustrates in a non-limiting manner examples of active or intermediate compounds according to the invention.

In the following table, M+H (or M-H) means the molecular ion peak, plus or minus 1 a.m.u. (atomic mass unit) respectively, as observed in mass spectroscopy and M (Apcl+) means the molecular ion peak as it was found via positive atmospheric pressure chemical ionisation in mass spectroscopy.

Example Z¹ T A M + H logP 1

cPr O

360 2

cPr O

348 3

cPr O

382 4

cPr S

398 5

cPr O

348 6

cPr O

314 7

cPr O

328 8

cPr O

344 9

cPr O

10

cPr O

370 11

cPr O

382 12

cPr O

328 13

cPr O

342 14

cPr O

15

cPr O

328 16

cPr O

406 17

cPr S

422 18

cPr O

19

cPr O

356 20

cPr O

21

cPr O

356 22

cPr O

386 23

cPr O

24

cPr O

329 25

cPr O

330 26

cPr O

346 27

cPr O

28

cPr O

364 29

cPr O

30

cPr O

406 31

cPr O

404 32

cPr O

502 33

cPr O

470 34

cPr O

405 35

cPr O

434 36

cPr O

378 37

cPr O

362 38

cPr O

400 39

cPr O

368 40

cPr O

382 41

cPr O

410 42

cPr O

382 43

cPr O

436 44

cPr O

402 45

cPr O

402 46

cPr O

460 47

cPr O

414 48

cPr O

398 49

cPr O

384 50

cPr O

400 51

cPr O

382 52

cPr O

396 53

cPr O

410 54

cPr O

420 55

cPr O

362 56

cPr S

378 57

cPr O

312 58

cPr O

326 59

cPr O

354 60

cPr O

326 61

cPr O

380 62

cPr O

346 63

cPr O

346 64

cPr O

404 65

cPr O

358 66

cPr O

342 67

cPr O

328 68

cPr O

344 69

cPr O

344 70

cPr O

326 71

cPr O

340 72

cPr O

354 73

cPr O

378 74

cPr O

366 75

cPr O

400 76

cPr O

366 77

cPr S

78

cPr O

332 79

cPr O

346 80

cPr O

362 81

cPr O

410 82

cPr O

388 83

cPr O

400 84

cPr O

346 85

cPr O

360 86

cPr O

87

cPr O

346 88

cPr O

424 89

cPr O

90

cPr O

374 91

cPr O

92

cPr O

374 93

cPr O

94

cPr O

95

cPr O

347 96

cPr O

348 97

cPr O

364 98

cPr O

436 99

cPr O

382 100

cPr O

101

cPr O

364 102

cPr O

520 103

cPr O

488 104

cPr O

376 105

cPr O

452 106

cPr O

424 107

cPr O

344 108

cPr O

402 109

cPr O

110

cPr O

111

cPr O

112

cPr O

113

cPr O

114

cPr O

115

cPr O

330 116

cPr O

388 117

cPr O

350 118

cPr O

364 119

cPr O

392 120

cPr O

364 121

cPr O

418 122

cPr O

384 123

cPr O

384 124

cPr O

442 125

cPr O

396 126

cPr O

380 127

cPr O

366 128

cPr O

382 129

cPr O

382 130

cPr O

364 131

cPr O

378 132

cPr O

392 133

cPr O

349 134

cPr O

363 135

cPr O

391 136

cPr O

363 137

cPr O

417 138

cPr O

383 139

cPr O

383 140

cPr O

441 141

cPr O

395 142

cPr O

379 143

cPr O

365 144

cPr O

381 145

cPr O

381 146

cPr O

363 147

cPr O

377 148

cPr O

391 149

cPr O

330 150

cPr O

151

cPr O

388 152

cPr O

395 153

cPr O

381 154

cPr O

401 155

cPr O

397 156

cPr O

367 157

cPr O

401 158

cPr O

381 159

cPr O

413 160

cPr O

459 161

cPr O

381 162

cPr O

399 163

cPr O

383 164

cPr O

399

Example Z¹ M + H logP 165

cPr 206 166

cPr 189 167

cPr 1.22 168

cPr 362 169

cPr 294 170

cPr 330 171

cPr 0.81 172

cPr 230 173

cPr 252 174

cPr 1.15 175

cPr 0.32 176

cPr 0.83 177

cPr 0.67 178

cPr 1.26

The following examples illustrate in a non-limiting manner the preparation and efficacy of the compounds of formula (I) according to the invention.

PREPARATION EXAMPLE N-(7-chloro-2,3-dihydro-1H-inden-1-yl)-N-cyclopropyl-5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide (compound 5)

Step 1: preparation of 7-chloro-N-cyclopropyl-2,3-dihydro-1H-inden-1-amine

To a cooled solution of 4.16 ml (60 mmol) of cyclopropylamine and 4.3 ml (75 mmol) of acetic acid, together with 5 g of 3A molecular sieves, in 80 ml of methanol, are added 5 g (30 mmol) of 7-chloro-2,3-dihydro-1H-inden-1-one. The reaction mixture is stirred for 4 hrs at reflux. The reaction mixture is then cooled to ambient temperature and 2.83 g (45 mmol) of sodium cyanoborohydride are slowly added. The reaction mixture is further stirred for 2 hrs at reflux. The solvent is removed under vacuum and 100 ml of water are then added to the residue and the pH is ajusted to 10 with sodium hydroxyde. The watery layer is extracted three times with dichloromethane (3×50 ml); the combined organic layers are dried over magnesium sulphate and concentrated in vacuum to yield 5.6 g (80% yield) of 7-chloro-N-cyclopropyl-2,3-dihydro-1H-inden-1-amine as an brown oil (M+1=208).

Step 2: preparation of N-(7-chloro-2,3-dihydro-1H-inden-1-yl)-N-cyclopropyl-5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide

At ambient temperature, a solution of 0.19 g (1.06 mmol) of 5-fluoro-1,3-dimethyl-1H-pyrazole-4-carbonyl chloride in 3 ml of tetrahydrofurane is added dropwise to a solution of 0.20 g (0.96 mmol) of 7-chloro-N-cyclopropyl-2,3-dihydro-1H-inden-1-amine and 0.15 ml triethylamine in 8 ml tetrahydrofurane. The reaction mixture is stirred for 3 hrs at reflux. The solvent is removed under vacuum and 10 ml of water are then added to the residue. The watery layer is extracted three times with ethyl acetate (3×20 ml); the combined organic layers are dried over magnesium sulphate and concentrated in vacuum. Column chromatography (gradient n-heptane/ethyl acetate) yields 0.26 mg (73% yield) of N-(7-chloro-2,3-dihydro-1H-inden-1-yl)-N-cyclopropyl-5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide as an orange oil (M+1=348).

GENERAL PREPARATION EXAMPLE Thionation of Amide of Formula (I) on Chemspeed Apparatus

In a 13 ml Chemspeed vial is weighted 0.27 mmole of phosphorous pentasulfide (P₂S₅). 3 ml of a 0.18 molar solution of the amide (I) (0.54 mmole) in dioxane is added and the mixture is heated at reflux for two hours. The temperature is then cooled to 80° C. and 2.5 ml of water are added. The mixture is heated at 80° C. for one more hour. 2 ml of water are then added and the reaction mixture is extracted twice by 4 ml of dichloromethane. The organic phase is deposited on a basic alumina cardridge (2 g) and eluted twice by 8 ml of dichloromethane. The solvents are removed and the crude thioamide derivative is analyzed by LCMS and NMR. Insufficiently pure compounds are further purified by preparative LCMS.

EXAMPLE A In Vivo Test on Pyrenophora teres (Barley Net Blotch)

The active ingredients tested are prepared by homogenization in a mixture of acetone/tween/DMSO, then diluted with water to obtain the desired active material concentration.

Barley plants (Express variety), sown on a 50/50 peat soil-pozzolana substrate in starter cups and grown at 12° C., are treated at the 1-leaf stage (10 cm tall) by spraying with the active ingredient prepared as described above. Plants, used as controls, are treated with the mixture of acetone/tween/DMSO/water not containing the active material.

After 24 hours, the plants are contaminated by spraying them with an aqueous suspension of Pyrenophora teres spores (12,000 spores per ml). The spores are collected from a 12-day-old culture. The contaminated barley plants are incubated for 24 hours at about 20° C. and at 100% relative humidity, and then for 12 days at 80% relative humidity.

Grading is carried out 12 days after the contamination, in comparison with the control plants. Under these conditions, good (at least 70%) or total protection is observed at a dose of 500 ppm with the following compounds: 1, 2, 3, 4, 5, 6, 8, 10, 11, 12, 13, 15, 16, 17, 19, 25, 28, 32, 35, 39, 40, 42, 43, 44, 45, 46, 47, 48, 49, 51, 52, 54, 55, 56, 62, 63, 64, 65, 69, 73, 74, 75, 76, 78, 79, 80, 81, 82, 83, 84, 85, 87, 90, 92, 95, 105, 117, 122, 125, 133, 134, 136, 137, 138, 139 and 141.

EXAMPLE B In Vivo Test on Mycosphaerella qraminicola (Wheat Leaf Spot)

The active ingredients tested are prepared by homogenization in a mixture of acetone/tween/DMSO, then diluted with water to obtain the desired active material concentration.

Wheat plants (Scipion variety), sown on a 50/50 peat soil-pozzolana substrate in starter cups and grown at 12° C., are treated at the 1-leaf stage (10 cm tall) by spraying with the aqueous suspension described above. Plants, used as controls, are treated with an aqueous solution not containing the active material.

After 24 hours, the plants are contaminated by spraying them with an aqueous suspension of Mycosphaerella graminicola spores (500 000 spores per ml). The spores are collected from a 7-day-old culture. The contaminated wheat plants are incubated for 72 hours at 18° C. and at 100% relative humidity, and then for 21 to 28 days at 90% relative humidity.

Grading (% of efficacy) is carried out 21 to 28 days after the contamination, in comparison with the control plants.

Under these conditions, good (at least 70%) or total protection is observed at a dose of 500 ppm with the following compounds: 1, 2, 3, 5, 6, 7, 8, 10, 15, 16, 19, 22, 24, 30, 31, 34, 35, 39, 40, 41, 42, 43, 44, 45, 46, 48, 49, 50, 51, 52, 53, 56, 57, 58, 59, 60, 62, 63, 65, 66, 68, 70, 72, 73, 74, 75, 76, 78, 80, 81, 83, 84, 87, 88, 90, 95, 102, 103, 105, 106, 107, 115, 116, 117, 118, 119, 121, 122, 123, 130, 131, 132, 133, 134, 136, 137, 138, 139, 140, 141, 142, 143, 144, 145, 146, 147, 148, 153 and 157.

EXAMPLE C In Vivo Test on Puccinia recondita (Brown Rust)

The active ingredients tested are prepared by homogenization in a mixture of acetone/tween/DMSO, then diluted with water to obtain the desired active material. Wheat plants (Scipion variety) sown on 50/50 peat soil-pozzolana substrate in starter cups and grown at 12° C., are treated at the 1-leaf stage (10 cm tall) by spraying with the aqueous suspension described above.

Plants, used as controls, are treated with an aqueous solution not containing the active material.

After 24 hours, the plants are contaminated by spraying the leaves with an aqueous suspension of Puccinia recondita spores (100,000 spores per ml). The spores are collected from a 10-day-old contaminated wheat and are suspended in water containing 2.5 ml/l of tween 80 10%. The contaminated wheat plants are incubated for 24 hours at 20° C. and at 100% relative humidity, and then for 10 days at 20° C. and at 70% relative humidity.

Grading is carried out 10 days after the contamination, in comparison with the control plants. Under these conditions, good (at least 70%) or total protection is observed at a dose of 500 ppm with the following compounds: 1, 2, 3, 4, 6, 7, 8, 10, 11, 12, 13, 15, 16, 17, 19, 22, 25, 26, 28, 30, 31, 33, 34, 35, 41, 42, 46, 47, 51, 53, 54, 55, 59, 65, 72, 73, 75, 84, 85, 87, 88, 90, 92, 96, 99, 101, 104, 106, 108, 116, 141, 149 and 151.

EXAMPLE D In Vivo Test on Alternaria brassicae (Leaf Spot of Crucifers)

The active ingredients tested are prepared by potter homogenization in a mixture of acetone/tween/water. This suspension is then diluted with water to obtain the desired active material concentration.

Radish plants (Pernot variety), sown on a 50/50 peat soil-pozzolana substrate in starter cups and grown at 18-20° C., are treated at the cotyledon stage by spraying with the active ingredient prepared as described above.

Plants, used as controls, are treated with the mixture of acetone/tween/water not containing the active material.

After 24 hours, the plants are contaminated by spraying them with an aqueous suspension of Alternaria brassicae spores (40,000 spores per cm³). The spores are collected from a 12 to 13 days-old culture.

The contaminated radish plants are incubated for 6-7 days at about 18° C., under a humid atmosphere.

Grading is carried out 6 to 7 days after the contamination, in comparison with the control plants. Under these conditions, good protection (at least 70%) is observed at a dose of 500 ppm with the following compounds: 2, 3, 4, 5, 7, 11, 12, 13, 17, 19, 25, 28, 31, 39, 40, 41, 42, 43, 44, 45, 47, 48, 51, 52, 53, 56, 65, 76, 79, 81, 82, 83, 85, 90, 92, 122, 138, 141 and 153.

EXAMPLE E In Vivo Iest on Botrytis cinerea (Grey Mould)

The active ingredients tested are prepared by homogenization in a mixture of acetone/tween/DMSO, then diluted with water to obtain the desired active material.

Gherkin plants (Vert petit de Paris variety), sown on a 50/50 peat soil-pozzolana substrate in starter cups and grown at 18-20° C., are treated at the cotyledon Z11 stage by spraying with the active ingredient prepared as described above.

Plants, used as controls, are treated with an aqueous solution not containing the active material. After 24 hours, the plants are contaminated by depositing drops of an aqueous suspension of Botrytis cinerea spores (150,000 spores per ml) on upper surface of the leaves. The spores are collected from a 15-day-old culture and are suspended in a nutrient solution composed of:

-   -   20 g/L of gelatin;     -   50 g/L of D-fructose;     -   2 g/L of NH₄NO₃;     -   1 g/L of KH₂PO₄.

The contaminated cucumber plants are settled for 5-7 days in a climatic room at 15-11° C. (day/night) and at 80% relative humidity.

Grading is carried out 5/7 days after the contamination, in comparison with the control plants.

Under these conditions, good (at least 70%) protection is observed at a dose of 500 ppm with the following compounds: 1, 2, 5, 6, 12, 15, 16, 39, 40, 42, 44, 45, 51, 74, 76, 78, 85, 133 and 138.

EXAMPLE F In Vivo Test on Sphaerotheca fuliginea (Powdery Mildew)

The active ingredients tested are prepared by homogenization in a mixture of acetone/tween/water. This suspension is then diluted with water to obtain the desired active material concentration.

Gherkin plants (Vert petit de Paris variety) in starter cups, sown on a 50/50 peat soil-pozzolana substrate and grown at 20° C./23° C., are treated at the cotyledon Z10 stage by spraying with the aqueous suspension described above. Plants, used as controls, are treated with an aqueous solution not containing the active material.

After 24 hours, the plants are contaminated by spraying them with an aqueous suspension of Sphaerotheca fuliginea spores (100 000 spores per ml). The spores are collected from a contaminated plants. The contaminated gherkin plants are incubated at about 20° C./25° C. and at 60/70% relative humidity.

Grading (% of efficacy) is carried out 12 days after the contamination, in comparison with the control plants.

Under these conditions, good (at least 70%) or total protection is observed at a dose of 500 ppm with the following compounds: 1, 2, 3, 5, 6, 7, 8, 12, 13, 15, 16, 17, 22, 24, 30, 39, 40, 41, 42, 43, 44, 45, 46, 48, 49, 50, 51, 52, 54, 56, 57, 59, 62, 64, 65, 66, 67, 70, 71, 72, 73, 74, 75, 76, 78, 80, 84, 85, 87, 92, 95, 96, 104, 106, 115, 117, 122, 123, 125, 130, 131, 133, 134, 135, 136, 138, 146 and 147.

EXAMPLE G In Vivo Test on Phakopsora pachyrhizi (Soybean Rust)

The active ingredients tested are prepared by homogenization in a mixture of acetone/Emulgator PS16. This suspension is then diluted with water to obtain the desired active material concentration.

Soybean plants (Miyagishirome variety), sown on a horticultural soil in plastic pots and grown at 20° C., are treated at the 1.5-leaf stage (20 cm tall) by spraying with the aqueous suspension described above. Plants, used as controls, are treated with an aqueous solution not containing the active material.

After 24 hours, the plants are contaminated by spraying them with an aqueous suspension of Phakopsora pachyrhizi spores (100,000 spores per ml). The spores are collected from contaminated plants. The contaminated soybean plants are incubated at about 20° C. and at 80% relative humidity.

Grading is carried out 11 days after the contamination, in comparison with the control plants. Under these conditions, good (at least 70%) or total protection is observed at a dose of 250 ppm with the following compounds: 1, 12, 13, 17, 19, 31, 90 and 92. 

1-16. (canceled)
 17. A compound of formula:

wherein Z¹ is selected from the group consisting of a non substituted C₃-C₇-cycloalkyl and a C₃-C₇ cycloalkyl substituted by up to 10 atoms or groups independently selected from the group consisting of halogen atoms; cyano; C₁-C₈-alkyl; C₁-C₈-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₈alkoxy; C₁-C₈-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkoxycarbonyl; C₁-C₈-halogenoalkoxycarbonyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkylaminocarbonyl; di-C₁-C₈-alkylaminocarbonyl; and carbamoyl; Z² is selected from the group consisting of a hydrogen atom; a halogen atom; cyano; C₁-C₈-alkyl; and C₁-C₈-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; L¹ and L² are independently selected from the group consisting of CZ⁴Z⁵, NZ⁶, O, S, S(O), and S(O)₂; m is 1, 2 or 3; X is selected from the group consisting of CZ⁷ and N; Z⁷ and each Z³ are independently selected from the group consisting of a hydrogen atom; a halogen atom; nitro; cyano; hydroxyl; thio; amino; pentafluoro-λ⁶-thio; C₁-C₈-alkyl; C₁-C₈-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkylamino; di-C₁-C₈-alkylamino; C₁-C₈-alkoxy; C₁-C₈-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkoxy-C₁-C₈-alkyl; C₁-C₈-alkylsulfanyl; C₁-C₈-halogenoalkylsulfanyl comprising up to 9 halogen atoms that can be the same or different; C₂-C₈-alkenyl; C₂-C₈-halogenoalkenyl comprising up to 9 halogen atoms that can be the same or different; C₂-C₈-alkynyl; C₂-C₈-halogenoalkynyl comprising up to 9 halogen atoms that can be the same or different; C₂-C₈-alkenyloxy; C₂-C₈-halogenoalkenyloxy comprising up to 9 halogen atoms that can be the same or different; C₂-C₈-alkynyloxy; C₂-C₈-halogenoalkynyloxy comprising up to 9 halogen atoms that can be the same or different; C₃-C₇-cycloalkyl; C₃-C₇-cycloalkyl-C₁-C₈-alkyl; C₃-C₇-halogenocycloalkyl comprising up to 9 halogen atoms that can be the same or different; formyl; formyloxy; formylamino; carboxy; carbamoyl; N-hydroxycarbamoyl; carbamate; (hydroxyimino)-C₁-C₈-alkyl; C₁ -C₈-alkylcarbonyl; C₁ -C₈-halogenoalkylcarbonyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkylcarbamoyl; di-C₁-C₈-alkylcarbamoyl; N—C₁-C₈-alkyloxycarbamoyl; C₁-C₈-alkoxycarbamoyl; N—C₁-C₈-alkyl-C₁-C₈-alkoxycarbamoyl; C₁-C₈-alkoxycarbonyl; C₁-C₈-halogenoalkoxycarbonyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkylaminocarbonyl; di-C₁-C₈-alkylaminocarbonyl; C₁-C₈-alkylcarbonyloxy; C₁-C₈-halogenoalkylcarbonyloxy comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkylcarbonylamino; C₁-C₈-halogenoalkylcarbonylamino comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkylaminocarbonyloxy; di-C₁-C₈-alkylaminocarbonyloxy; C₁-C₈-alkyloxycarbonyloxy; C₁-C₈-alkylsulfenyl; C₁-C₈-halogenoalkylsulfenyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkylsulfinyl; C₁-C₈-halogenoalkylsulfinyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkylsulfonyl; C₁-C₈-halogenoalkylsulfonyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkoxyimino; (C₁-C₈-alkoxyimino)-C₁-C₈-alkyl; (C₁-C₈-alkenyloxyimino)-C₁-C₈-alkyl; (C₁-C₈-alkynyloxyimino)-C₁-C₈-alkyl; a (benzyloxyimino)-C₁-C₈-alkyl; tri(C₁-C₈-alkyl)silyl; tri(C₁-C₈-alkyl)silyl-C₁-C₈-alkyl; phenyl that can be substituted by up to 5 groups Q; benzyloxy that can be substituted by up to 5 groups Q; benzylthio that can be substituted by up to 5 groups Q; benzylamino that can be substituted by up to 5 groups Q; naphthyl that can be substituted by up to 6 groups Q; phenoxy that can be substituted by up to 5 groups Q; phenylamino that can be substituted by up to 5 groups Q; phenylthio that can be substituted by up to 5 groups Q; phenylmethylene that can be substituted by up to 5 groups Q; pyridinyl that can be substituted by up to four groups Q; pyridinyloxy that can be substituted by up to four groups Q; and phenoxymethylene that can be substituted by up to 5 groups Q; or two substituents Z³ or Z⁷ together with the consecutive carbon atoms to which they are linked can form a 5- or 6-membered, saturated or non-saturated, carbo- or hetero-cycle, that can be substituted by up to four groups Q that can be the same or different; p is 1, 2, or 3; Z⁴ and Z⁵ are independently selected from the group consisting of a hydrogen atom; a halogen atom; cyano; nitro; C₁-C₈-alkyl; C₁-C₈-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkoxy; C₁-C₈-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkoxy-C₁-C₈-alkyl; C₂-C₈-alkenyl; C₂-C₈-halogenoalkenyl comprising up to 9 halogen atoms that can be the same or different; C₂-C₈-alkynyl; C₂-C₈-halogenoalkynyl comprising up to 9 halogen atoms that can be the same or different; C₃-C₇-cycloalkyl; C₃-C₇-cycloalkyl-C₁-C₈-alkyl; C₃-C₇-halogenocycloalkyl comprising up to 9 halogen atoms that can be the same or different; formyl; C₁-C₈-alkylcarbonyl; C₁-C₈-halogenoalkylcarbonyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkylsulfanyl; C₁-C₈-halogenoalkylsulfanyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkylsulfinyl; C₁-C₈-halogenoalkylsulfinyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkylsulfonyl; and C₁-C₈-halogenoalkylsulfonyl comprising up to 9 halogen atoms that can be the same or different; Z⁶ is selected from the group consisting of a hydrogen atom; C₁-C₈-alkyl; C₁-C₈-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkoxy-C₁-C₈-alkyl; C₂-C₈-alkenyl; C₂-C₈-halogenoalkenyl comprising up to 9 halogen atoms that can be the same or different; C₂-C₈-alkynyl; C₂-C₈-halogenoalkynyl comprising up to 9 halogen atoms that can be the same or different; C₃-C₇-cycloalkyl; C₃-C₇-cycloalkyl-C₁-C₈-alkyl; C₃-C₇-halogenocycloalkyl comprising up to 9 halogen atoms that can be the same or different; formyl; C₁-C₈-alkylcarbonyl; C₁-C₈-halogenoalkylcarbonyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkylsulfonyl; C₁-C₈-halogenoalkylsulfonyl comprising up to 9 halogen atoms that can be the same or different; phenylsulfonyl can be substituted by up to 5 groups Q; and benzyl that can be substituted by up to 5 groups Q; each Q is independently selected from the group consisting of a halogen atom; cyano; nitro; C₁-C₈-alkyl; C₁-C₈-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkoxy; C₁-C₈-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkylsulfanyl; C₁-C₈-halogenoalkylsulfanyl comprising up to 9 halogen atoms that can be the same or different; tri(C₁-C₈)alkylsilyl; and tri(C₁-C₈)alkylsilyl-C₁-C₈-alkyl; provided that: (A) X represents N when Z⁴ and Z⁵ are both hydrogen or when L² is NZ⁶; and (B) the compound is not 3-(cyclopropylamino)-2,3-dihydro-1,7-dimethyl-1H-indan-4-ol.
 18. The compound of claim 17 wherein Z¹ is a cyclopropyl.
 19. The compound of claim 17 wherein Z¹ is a non-substituted cyclopropyl.
 20. The compound of claim 17 wherein Z² is a hydrogen atom.
 21. The compound of claim 17 wherein L¹ is CZ⁴Z⁵.
 22. The compound of claim 17 wherein L² is CZ⁴Z⁵ and m is 1 or
 2. 23. The compound of claim 17 wherein Z⁷ and each Z³ are independently selected from the group consisting of a hydrogen atom; a halogen atom; C₁-C₈-alkyl; C₁-C₈-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; C₁-C₈-alkoxy; and C₁-C₈-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different. 